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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1761451Generated: November 3, 2026

HCID 131715934, compound → HCID 21241513, compound

https://huagongshe.com/reaction/1761451

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 131715934HCID 131715934—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductHCID 21241513HCID 21241513—

Reaction Steps

A solution of 1-[1-(4-methoxyphenyl)-3-[4-(phenylmethyl)-1-piperazinyl]-1-propenyl]cyclohexanol, dihydrochloride (14.6 g, 29.6 mmole) in ethanol (250 mL) was hydrogenated in a Parr apparatus over 10% Pd/C for 65 hours. The catalyst was filtered and the filtrate evaporated. The residue was partitioned between ethyl acetate (120 mL) and N sodium hydroxide (65 mL). The layers were separated. The aqueous phase was extracted with ethyl acetate. The combined organic solution was washed with brine, dried over magnesium sulfate and evaporated to obtain the title compound as an oil. Wt. 7.8 g. Mass spectral analysis: Molecular weight by C.I.M.S.: M+1 334.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04826844
Source datasetuspto-grants-1989_05
ORD IDord-2790ad0c4be84b11ae9eab226f137c55
Source noteuspto-grants-1989_05